Reactive polymeric lost circulation materials

Patent metadata

Field	Value
Publication number	US-11326089-B2
Application number	US-201916652297-A
Country	US
Kind code	B2
Filing date	May 20, 2019
Priority date	May 20, 2019
Publication date	May 10, 2022
Grant date	May 10, 2022

Abstract

Compositions and methods involving polyvalent cation reactive polymers for use as lost circulation materials in subterranean treatment operations are provided. In some embodiments, the methods include forming a treatment fluid including a base fluid, a source of a polyvalent cation, a polyvalent cation reactive polymer, and an acid precursor; introducing the treatment fluid into a wellbore penetrating at least a portion of a subterranean formation; and allowing the treatment fluid to at least partially set.

First claim

What is claimed is:

1. A method comprising:
forming a treatment fluid comprising
a base fluid,
a source of a polyvalent cation comprising at least one of an acid-soluble mineral fiber or a salt selected from the group consisting of: calcium carbonate, calcium sulfate-hydrate, magnesium carbonate, calcium oxide, magnesium oxide, calcium hydroxide, magnesium hydroxide, barium sulfate, or any combination thereof,
a polyvalent cation reactive polymer, and
an acid precursor;
introducing the treatment fluid into a wellbore penetrating at least a portion of a subterranean formation;
allowing the acid precursor to at least partially degrade and release one or more acids;
allowing the one or more acids to at least partially degrade or dissolve the source of the polyvalent cation to release one or more polyvalent cations; and
allowing the one or more polyvalent cations to crosslink at least a portion of the polyvalent cation reactive polymer; and
allowing the treatment fluid to at least partially set.

2. The method of claim 1 , wherein the at least partially set treatment fluid at least partially plugs a loss zone in the subterranean formation.

3. The method of claim 1 , wherein the source of the polyvalent cation comprises particles sized within a range of from about 1 to about 2,000 microns in diameter or fibers with a diameter of from about 1 micron to about 20 microns and a length of from about 1 micron to about 25,000 microns.

4. The method of claim 1 , wherein the source of the polyvalent cation comprises an acid-soluble mineral fiber.

5. The method of claim 1 , wherein the polyvalent cation reactive polymer is selected from the group consisting of: carrageenan, pectin, algin, alginate, carboxymethylcellulose, carboxymethyl hydroxypropyl guar, carboxymethyl hydroxyethyl guar, xanthan, diutan, carboxymethylhydroxylcellulose, carboxymethyl starch, partially hydrolyzed polyacrylamide, polyacrylic acid, polyacrylate any derivative of the foregoing, and any combination thereof.

6. The method of claim 1 , wherein the treatment fluid does not include a significant amount of particles sized greater than 1,000 microns in diameter.

7. The method of claim 1 , wherein the source of the polyvalent cation is present in the treatment fluid in an amount within a range of from about 0.01% to about 20% by weight of the treatment fluid.

8. The method of claim 1 , wherein the polyvalent cation reactive polymer is present in the treatment fluid in an amount within a range of from about 0.01% to about 40% by weight of the treatment fluid.

9. The method of claim 1 , wherein the acid precursor is present in the treatment fluid in an amount within a range of from about 0.01% to about 20% by weight of the treatment fluid.

10. The method of claim 1 , wherein the treatment fluid is introduced into the wellbore using one or more pumps.

11. The method of claim 1 , wherein the crosslinking of the polyvalent cation reactive polymer causes the treatment fluid to at least partially set.

12. A method comprising:
forming a treatment fluid comprising an aqueous base fluid, calcium carbonate, a polyvalent cation reactive polymer comprising alginate, and an acid precursor;
introducing the treatment fluid into a wellbore penetrating at least a portion of a subterranean formation;
allowing the acid precursor to at least partially degrade and release one or more acids;
allowing the one or more acids to at least partially degrade or dissolve the source of the polyvalent cation to release one or more polyvalent cations; and
allowing the one or more polyvalent cations to crosslink at least a portion of the polyvalent cation reactive polymer; and
allowing the treatment fluid to at least partially set.

13. The method of claim 12 , wherein the at least partially set treatment fluid at least partially plugs a loss zone in the subterranean formation.

14. The method of claim 12 , wherein the calcium carbonate comprises particles sized within a range of from about 1 to about 2,000 microns in diameter.

15. The composition of claim 12 , wherein the acid precursor is selected from the group consisting of: a lactone, a lactide, an acetate ester, a formate ester, a lactate ester, a polyester, an orthoester, or any combination thereof.

16. The method of claim 12 , wherein the treatment fluid does not include a significant amount of particles sized greater than 1,000 microns in diameter.

17. A method comprising:
forming a treatment fluid comprising an aqueous base fluid, calcium carbonate, a polyvalent cation reactive polymer comprising alginate, and a formic acid precursor;
introducing the treatment fluid into a wellbore penetrating at least a portion of a subterranean formation comprising a loss zone;
allowing the acid precursor to at least partially degrade and release one or more acids;
allowing the one or more acids to at least partially degrade or dissolve the source of the polyvalent cation to release one or more polyvalent cations; and
allowing the one or more polyvalent cations to crosslink at least a portion of the polyvalent cation reactive polymer;
allowing the treatment fluid to at least partially set, wherein the at least partially set treatment fluid at least partially plugs the loss zone; and
allowing the at least partially set treatment fluid to at least partially degrade or dissolve.

18. The method of claim 17 , wherein the source of the polyvalent cation comprises particles sized within a range of from about 1 to about 2,000 microns in diameter or fibers with a diameter of from about 1 micron to about 20 microns and a length of from about 1 micron to about 25,000 microns.

Assignees

• Halliburton Energy Services Inc

Inventors

• May Preston Andrew
• Zhou Hui
• Deville Jay

Classifications

• C04B2103/0067

  the ingredients being formed in situ by chemical reactions or conversion of one or more of the compounds of the composition · CPC title

• C09K8/512

  containing cross-linking agents · CPC title

• C09K8/035

  Organic additives · CPC title

• C09K8/514 Primary

  of natural origin, e.g. polysaccharides, cellulose (C09K8/512 takes precedence) · CPC title

• C04B26/28

  Polysaccharides or derivatives thereof · CPC title